Pediatric Hospice Palliative Care. Guiding Principles and Norms of Practice

Transcription

1 Pediatric Hospice Palliative Care Guiding Principles and Norms of Practice March 2006

2 Production of this document has been supported by a financial contribution from the Primary and Continuing Care Division, Health Care Policy Directorate, Health Canada through the Secretariat on Palliative and End-of-Life Care. Please note that the views expressed herein do not necessarily represent the official policy of Health Canada. Canadian Hospice Palliative Care Association Annex B, Saint-Vincent Hospital 60 Cambridge Street North Ottawa, Ontario, Canada K1R 7A5 Phone: (613) Toll-free in Canada: (800) Fax: (613) info@chpca.net Web Site: Copyright 2006, Canadian Hospice Palliative Care Association. All Rights Reserved. 1

3 Table of Contents Preface 4 Acknowledgements 6 Background 7 What is pediatric hospice palliative care? 7 How does hospice palliative care for children differ from hospice palliative care for adults? 7 What is the role of pediatric hospice palliative care during illness? 9 Guiding Principles of Pediatric Hospice Palliative Care 10 The Square of Care: a Conceptual Framework 12 I. Child and Family Care Illness/Disease Management Physical Care (including pain and symptom management) Psychosocial Care Social Care Spiritual Care Developmental Care Practical Care End of Life/Preparation for Death Care Loss, Grief, Bereavement Care 27 II. The Process of Providing Care Assessment Information-sharing Decision-making Therapeutic Interventions Care Delivery Evaluation of Care 37 2

4 III. Program Support Functions Governance and Administration Planning Marketing and Advocacy Quality Management Research Education Caregiver Support/Worklife 44 IV. Resources Human, Physical, Technology, Clinical Resources Financial Resources 46 Appendix A Glossary of Commonly Used Terms 47 Appendix B Informed Consent 50 Appendix C Cultural Care 51 Appendix D Techniques for Negotiating Issues Influenced by Culture that are Important in End of Life Care 52 Appendix E Bereavement Risk Assessment 55 Appendix F Quality Management 57 Appendix G Research Priorities and Questions 58 References 61 3

5 Preface In Canada, in a geographical area with 250,000 people and a child population of about 50,000, about 50 children are likely to have a life threatening condition and, at any given time, about half of those children will need hospice palliative care. Each year, about 5 will die from a lifethreatening illness (Goldman, 1998). Although the number of childhood deaths each year may seem small, the emotional, social and financial impact is extraordinary. A child s death is a painful, sorrowful loss for parents, siblings, extended family members, teachers, health care caregivers, volunteers and others. During the dying journey, children and their families suffer from reduced quality of life, loss of family income, inconsistency in the availability and quality of hospice palliative care, and the lack of true choices about where the child dies (75% to 80% of deaths among children in Canada occur in hospital intensive care units which may not be the first choice for children and families). The practice of hospice palliative care, which began in the 1970s, is designed to enhance choice, relieve suffering, and ensure the best quality of care during living, dying and grieving. Until recently, hospice palliative care had focused predominantly on the needs of adults who are dying, and the needs of children have been overlooked. This is changing. Groups such as Children s International Palliative Projects and Services (ChIPPS) and the Canadian Hospice Palliative Care Association Pediatric Interest Group [Canadian Network of Palliative Care for Children (CNPCC)] have brought together leaders in the field to share ideas and advance the field of pediatric hospice palliative care. Children with life threatening conditions and their families have the right to receive hospice palliative care that is planned, coordinated and delivered by formal caregivers who understand how to enhance a child s quality of life. Over the past year, the CHPCA s Canadian Network of Palliative Care for Children (CNPCC) have worked to adapt the Canadian Hospice Palliative Care Association's (CHPCA) national principles and norms of practice for pediatric care. How to Use this Document This document is designed to guide health care professionals in establishing standards of practice, service delivery, program and policies for pediatric hospice palliative care, regardless of whether that care is delivered at home, in a hospital, in a long term care facility, or in a hospice. Its goal is to promote a standard consistent approach to pediatric hospice palliative care in Canada. A standard approach to pediatric hospice palliative care will help to: ensure all families have access to high quality care make formal caregivers and organization more effective at identifying family issues, the care required, and the resources required to provide that care ensure all caregivers are knowledgeable and skilled, and have the support they need to fulfill their roles identify any gaps in care and encourage formal caregivers to expand their services or develop partnerships with other caregivers to fill the gaps. 4

6 Everyone providing pediatric hospice palliative care is encouraged to use the principles and norms set out in this document to guide their activities. Norms are simple statements that describe the usual or normal practice. Pediatric hospice palliative care programs use that statement to develop more detailed, measurable standards. For example, the norm for assessing a child and family s need for pediatric hospice palliatives care is a fairly general statement: Assessment is comprehensive and timely so clinicians have adequate information to guide the plan of care. An organization would then establish minimum standards that formal caregivers must meet to achieve that norm. For example: The assessment will be done using (name of assessment form). All questions must be completed. The assessment will be done within 24 hours of the child being referred to the program. While working from common principles and norms encourages consistency, it doesn t imply uniformity. Organizations will differ in the way they develop and function, and in the policies, procedures and strategies they develop to guide their practice. 5

7 Acknowledgements The CHPCA s Canadian Network of Palliative Care for Children (CNPCC) would like to acknowledge the many people who contributed to developing this document, including: the CHPCA Standards Committee, the group that developed A Model to Guide Hospice Palliative Care: Based on National Principles and Norms of Practice, which formed the basis for this document the Pediatric Hospice Palliative Care Committee of British Columbia. B.C. Children s Hospital and Canuck Place Children s Hospice in B.C., who provided expertise in pediatric palliative care the Pediatric Hospice Palliative Care Standards Committee at the Hospital for Sick Children in Toronto who provided expertise in pediatric palliative care members of the CHPCA s Canadian Network of Palliative Care for Children (CNPCC) 6

8 Background What is pediatric hospice palliative care? Pediatric hospice palliative care is an active, holistic approach to care which focuses on relieving the physical, social, psychological and spiritual suffering experienced by children and families who face a progressive, life-threatening condition, and helping them fulfill their physical, psychological, social and spiritual goals. Its philosophy is to provide optimal comfort and quality of life, and sustain hope and family connection despite the likelihood of death. Pediatric hospice palliative care aims to provide comprehensive care for children and their families through the living, dying and grieving processes. It affirms life and regards dying as a process that is a profoundly personal experience for the child and family. Pediatric hospice palliative care is planned and delivered collaboratively by an interdisciplinary team. It is a child and family centred approach to care that is based on shared decision-making and sensitivity to the family s cultural and spiritual values, beliefs and practices. (Adapted from the Canadian Hospice Palliative Care Association, and Precepts of Palliative Care for Children/Adolescents and Their Families, 2003). How does hospice palliative care for children differ from hospice palliative care for adults? Pediatric hospice palliative care is based on the same principles as adult hospice palliative care but also recognizes the unique needs of families faced with a child s illness and death. Children and adolescents are in a process of physical, emotional, cognitive and spiritual development. Depending on their developmental stage, they have different skills and different emotional, physical and development issues/needs. Children and adolescents communicate differently, and their understanding of illness, death and dying depends on their stage of development. Health care professionals understand that a child s concepts of illness and dying continue to evolve over time, and develop in association with life and illness experience (Bluebond-Langner, 1978; Eiser, 1995). Religious/cultural beliefs, patterns of coping, disease experience, previous experience with loss/death, sadness, and other emotions associated with grief, all influence a child s understanding of death (Eiser, 1995; McConnell & Frager, 2003; Work Group on Palliative Care for Children, 1999; Committee on Bioethics and Committee on Hospital Care, 2000). Children are members of many communities, including families, neighbourhoods and schools, and their continuing role in these communities should be incorporated into their 7

9 dying journey. School is an integral part of their lives, and it is essential they have ongoing opportunities to pursue education. Children respond differently to therapies and drugs. They experience unique symptoms, such as fatigue, nausea, vomiting and shortness of breath, depression and anxiety which are not well understood. They experience and express pain differently than adults, and require individualized treatment. Children are not as able to advocate for themselves, and often rely on family members to make decisions for them. Many life-threatening conditions that affect children are rare and only affect children. Many of the illnesses are familial and may affect more than one child in the family. The diseases are often unpredictable in terms of prognosis, and children may require years of caregiving. Parents bear a heavy responsibility for the care of their child, which may include making decisions in the best interest of the child at a time when they are highly stressed and grieving the loss of their child s health as well as dealing with other losses such as financial stability and the loss of time to spend with other children. Families of children who have lifethreatening conditions tend to be younger and have fewer resources. Their quality of life is significantly improved when the ill child s quality of life is enhanced. The grief associated with a child s death has devastating, long-term implications for the entire family. Siblings have unique needs during and after a child s death. 8

10 What is the role of pediatric hospice palliative care during illness? Pediatric hospice palliative care may be combined with therapies designed to reduce or cure illness, or it may be the only focus of care. Figure 1shows the relative focus of care over time. The straight dashed line is used to distinguish therapies intended to modify disease from those that are intended to relieve suffering and/or improve the quality of life (i.e., hospice palliative care). The actual mix of concurrent therapies will vary for each child/family care situation based on their expectations and needs, goals of care, and treatment priorities. Figure 1: The Role of Pediatric Hospice Palliative Care F o c u s o f C a r e P r e s e n t a t i o n Curative therapy to modify disease and to relieve suffering Grief and loss support Therapy to relieve suffering and/or improve quality of life Bereavement Care Death Diagnosis Illness Experience End of Life Care Pediatric hospice palliative care should be available to children and families throughout their illness experience and beyond, whenever they have expectations and needs and are prepared to accept care. Pediatric hospice palliative care is appropriate for any pediatric patient and/or family living with a life-threatening condition due to any diagnosis. Formal caregivers work with other professionals, the child and family to provide pediatric hospice palliative care concurrently with active care. Although the child s care may focus more on palliation as the illness progresses, active treatment is part of hospice palliative care and both play an important role throughout a child s illness. 9

11 Guiding Principles of Pediatric Hospice Palliative Care Pediatric hospice palliative care is guided by the same values and principles as adult hospice palliative care (see a Model to Guide Hospice Palliative Care). In addition, pediatric hospice palliative care reflects the following principles. 1. Child/Family Focused Care The unit of care is the family, defined as the persons who provide physical, psychological, spiritual and social comfort to the child, and who are close in knowledge, care and affection -- regardless of genetic relationships. Family members may include biological, marital, adoptive/custodial and family of choice ties/connections (including friends and pets). Children and families facing illness, dying and bereavement have inherent strengths. As part of the process of providing pediatric hospice palliative care, formal caregivers explore the child s/family s needs, hopes, beliefs, fears, expectations and strengths. All aspects of care are provided in a manner that is sensitive to the child s and family s personal, cultural and spiritual values, beliefs and practices, their developmental stage, and their preparedness to deal with the dying process. The child has the right to age-appropriate information about his/her illness, potential treatments and outcomes. The family and service providers have the right to be informed about the illness, potential treatments and outcomes, while respecting the child s right to confidentiality. Decisions are made by the child and family in collaboration with the formal caregivers and service providers. The care team respects the child s and family s choices. 2. The Value of the Therapeutic Relationship A therapeutic relationship between health care professionals and the child/family is essential to the provision of pediatric hospice palliative care. Within this relationship, there is potential for healing in the midst of illness, death and bereavement. 3. Continuity of Care Pediatric hospice palliative care strives to provide continuity of care among formal and informal caregivers, and across the continuum of illness, dying and bereavement. 4. Communication Effective supportive pediatric hospice palliative care depends on the ability of the child/family and the palliative care team to communicate. Formal caregivers acknowledge and respect the 10

12 child s/family s language preference. Interpreter services are used, whenever possible, to meet the care unit s communication needs 5. Accessibility Pediatric hospice palliative care is accessible to children and their families in a setting of their choice that is appropriate to their needs and resources. Pediatric hospice palliative care is available 24 hours a day, 7 days a week, and families have a contact person to help coordinate their care. Ethical Considerations in Pediatric Hospice Palliative Care In their efforts to provide child/family-centred care, pediatric hospice palliative care providers will face a number of ethical issues including: the child s ability to consent to treatment. Some provinces have established specific ages at which a child is able to consent to treatment. Others require that the child be capable of understanding the treatment being proposed, the benefits and risks, and alternatives, and make the decision without coercion. Emphasizing the competence or capacity of the child rather than age, allows children to participate in decisions regarding their care whenever possible and appropriate. However, not having a legal age of consent can cause parents and professionals to question how much responsibility or information a child should be given in his or her own treatment decisions. the amount/type of information that should be shared with a child (i.e., truth telling). Honest and sensitively communicated medical information helps patients and their families understand and deal with health issues and make informed choices about care options (Brinchmann, Fǿrde & Nortvedt; Hébert, 1996; Charlton, 1996; Hébert, Hoffmaster, Glass & Singer, 1999; Kuhl, 2002). When, what and how to disclose information to children must take into account the family s cultural or religious values and the child s capacity to understand. The significance of and approach used for truth-telling, is strongly tied to an individual s or family s religious and cultural practices and values. A child also has the right to waive the option of receiving this information, preferring instead that parents receive information on his or her behalf. If the health care team and the family cannot agree on the information to be shared with the child, the team should consult with an ethicist. family-focused decision making. Decisions regarding the medical care of children are generally made in a triadic model which involves the participation of the child (according to child s ability and capacity), the child s parents and the health care team (Hardart, 2000; Harrison, Kenny, Sidarous & Rowell, 1999). In end of life care, decision making can be perceived by some families as profoundly burdensome if the primary responsibility for choosing among care options is placed on the parents at a time in which they are losing their child (Brinchmann, Fǿrde & Norvedt, 2002). Therefore, the role and participation of the health care team is crucial to imparting information, making recommendations and working collaboratively to reach a consensus on what is in the best interests of the child. With infants and young children, who have no significant decision-making capacity, parents and health care professionals should make decisions that are guided by the best interests of the child. With primary school children, who have some capacity, parents and professionals should provide age-appropriate information, seek the child s consent, take into consideration the 11

13 child s dissent, and ensure the child s best interests are at the core of the decisions. With adolescents, who have greater capacity, care must be taken to determine whether a particular adolescent patient has the ability to understand and communicate relevant medical information, exercise independence, anticipate consequences or risks and demonstrate a stable set of values (Harrison et al., 1999). All decision making should be sensitive to the child s and family s cultural and religious values. It s important that professionals understand how the family s cultural or religious beliefs shape understanding of illness and death. If a conflict arises between the health care caregivers and the child s family about the child s participation in his or her own care, health care caregivers should enlist the assistance of a cultural interpreter, chaplain or ethicist. Pediatric hospice palliative care programs should also have an established process of conflict resolution. pain management. Health professionals providing pediatric hospice palliative care have an ethical duty to pursue comfort aggressively and minimize the child s discomfort, suffering or pain (Wolfe, 2000). They have an ethical responsibility to provide adequate pain control and ensure that children are not under-treated because of ethical confusion, fear of the law or ignorance (Wolfe, 2000). The ethical obligations of beneficence, non-maleficence and the promotion of best interests of the patient should be used in guiding pain management decisions for children at end of life. decisions to forego potentially life-sustaining treatments or to withdraw life support. During the process of end of life care, health care professionals and parents will discuss foregoing life-sustaining treatment or withdrawing life support, and may participate in making these profoundly difficult decisions. To meet the requirements of non-malficence (i.e., the duty to avoid harm or suffering), professionals must raise these issues sensitively (i.e., identify appropriate timing, and present their recommendations to parents in a sensitive and respectful way). These conversations require comfortable rooms that afford privacy, as well as sufficient time for the family to ask questions, discuss preferences, voice objections and express feelings. These decisions, like all other decisions in pediatric hospice palliative care, should be driven by the best interests of the child. It is important to consider the child s values, beliefs and wishes as well as the options that are least likely to cause more suffering and/or prolong the dying process. It is also important to ensure that the self-interests of the parent(s) or over-riding familial interests do not dominate the decision-making. The Square of Care: a Conceptual Framework The conceptual framework for hospice palliative care is known as the Square of Care (see A Model to Guide Hospice Palliative Care), which captures the inter-relationship between clinical and program activities. The Square of Care developed for adult hospice palliative care has been adapted to guide pediatric hospice palliative care. The Square of Care for pediatric hospice palliative care consists of: the child and family, the unit of care, who are at the centre of the square the clinical activities involved in pediatric hospice palliative care, which include: Child and Family Care: the types or domains of care the child/family may need, such as disease management, physical care, spiritual care -- shown on the left side of the square 12

14 the Process of Providing Care: the steps health professionals use to provide the domains of care, such as assessment, decision making, care delivery shown on the top of the square the operational activities that support effective pediatric hospice palliative care, which include: program support functions, such as planning, marketing, education and research shown on the right side of the square governance and administration, including resources, information technology and organizational structure shown on the bottom of the square. The Square of Care for pediatric hospice palliative care (next page) illustrates: 1. The relationship of each of the domains of child and family care with the process of providing care 2. The relationship of each of the domains in Governance and Administration to each of the domains within Program Support. 3. The relationship of each activity to the child and family (who bring their own characteristics, such as age, gender, ethnicity, race, education, literacy). 4. The supportive role that program operations (Governance and Administration, and Program Support) play in the clinical activities (Child and Family Care, and the Process of Providing Care). This document sets out the principles and norms of practice for: Child and Family Care the Process of Providing Care Program Support Functions. 13

15 Figure 2: The Square of Care (Ferris et al, 2002) History, Physical examination Laboratory tests Diagnostic studies Assessment Confidentiality, Communication, Translation Information Sharing Goals of care, Treatment priorities, Withholding, Withdrawing therapy, Advance care planning, Capacity, Futility Requests for hastened death Decision Making Medications, Therapies, including integrative therapies, Equipment, Supplies, Benefits, risks, burdens, Adverse effects, Interactions, Education Therapeutic Interventions Access, Response times, Care planning Interdisciplinary team Collaboration Essential services Coordination Resources, Discrimination/prejudice Continuity, Safety, Consultation Care Delivery Evaluation Ongoing Clinical Care Evaluation of Care Diagnosis Prognosis Disease-modifying therapies IIllness/Disease Management PROCESS OF PROVIDING CARE Pain, other symptoms Function Fluids/nutrition Senses Emotion Coping responses Cognition, affect, depression, anxiety Independence, control Fears, sense of burden Dignity Family, friends, relationships Environment/safety Privacy, intimacy Financial, legal Meaning, value Existential Transcendental Faith, religion School and education Developmental milestones Family issues -Parents -Siblings -Child Activities of daily living Caregiving Caregiver training, support Life closure, gift giving Legacy creation Rites, rituals, celebrations, funerals Last hours of living Loss Anticipatory, acute and chronic grief Bereavement Physical Psychological Social Planning Practical End of Life/ Preparation for Death Loss, Grief, Bereavement C H I L D & F A Spiritual M Marketing and Advocacy I L Developmental Y Quality Management C A R E Child / Family Fixed Characteristics: Age, gender, ethnicity, race education, literacy Funding Caregiver Support/ Worklife Education Research GOVERNANCE & ADMINISTRATION - Vision, mission, values, norms of practice - Communication and information technology - Organizational structure Safety, security, emergency systems - Human resources -Financial accountability - Space and environment - Legal, regulatory compliance - Medical and office equipment - Diagnostic, therapeutic services - Health records 14

16 I. Child and Family Care Child and family care consists of 9 types or domains of care, including: illness/disease management physical care (including pain and symptom management) psychosocial care social care spiritual care developmental care practical care end of life, preparation for death care loss, grief and bereavement care. 1. Illness/Disease Management Principle PP1.1 Children and families have access to appropriate illness-modifying therapy. PP1.2 Children and families have access to information on the impact of illness-modifying therapy on quality of life. PP1.2 Children and families have access to supports to help overcome any barriers to accessing appropriate illness-modifying therapy (e.g., travel costs, child care for siblings, loss of work income). Norms of Practice PN1.1 PN1.2 Each member of the family, including the child and siblings (when possible taking into account the children s developmental milestones and the family s cultural beliefs) understands the child s diagnoses. Formal caregivers estimate the child s prognosis based on best available evidence when possible. 15

17 PN1.3 PN1.4 PN1.5 PN1.6 Formal caregivers appropriately communicate the meaning and implications of the estimated prognosis with the child and family, taking into account the child s age and stage of development and the family s cultural values, and without destroying hope. Formal caregivers use appropriate language with children and families, including clear language related to dying and death, to minimize misconceptions and facilitate discussions to help prepare children and families for end of life. Formal caregivers know the child s history of therapeutic interventions and their effectiveness, resolved and unresolved issues, and adverse events. Formal caregivers offer the child/family illness-modifying therapy that is appropriate to the child s/family s goals of care and has the potential to relieve the child s suffering and/or improve quality of life without disproportionate risk or burden. 16

18 2. Physical Care (including pain and symptom management) Principles PP2.1 PP2.2 PP2.3 PP2.4 PP2.5 Symptoms include emotional and spiritual distress, such as boredom, depression, loneliness and sadness, as well as physical suffering. Effective symptom management addresses physical, cognitive, emotional, psychosocial and spiritual symptoms in order to ease the total pain a child and family experiences. Pain and other symptoms are managed effectively to achieve the greatest possible relief for the child and family. Age, cognitive ability, illness trajectory, cultural values and previous experience with pain/symptoms can affect a child s perception and experience of pain/symptoms, as well as the family s perception of the child s pain. Alternative and complementary therapies for pain and symptom management are accepted methods of healing when chosen by the child and family, unless they are likely to cause significant harm. Access to pain management expertise/leaders is available 24 hours a day, 7 days a week. Norms of Practice PN2.1 PN2.2 PN2.3 Formal caregivers assess specific patient and family needs related to pain and symptom management. Assessment is ongoing and based on age appropriate and valid assessment tools. The plan of care addresses the physical expectations and needs of the child and family, and includes an effective pain and symptom management plan as well as plans for appropriate management of potential pharmacological side effects and complications. Commonly addressed symptoms include but are not limited to: cardio-respiratory symptoms (e.g., respiratory distress/failure, cough, edema, hiccups) gastrointestinal symptoms (e.g., nausea, vomiting, constipation, obstipation, bowel obstruction, diarrhea, feeding intolerance) general symptoms (e.g., anorexia, cachexia, fatigue, bleeding, odour, pruritus, infection, skin breakdown) neurological symptoms (e.g., seizures, level of consciousness, mobility, weakness, muscle spasms, swallowing, speech, body alignment and contractures) psychological and psychosocial symptoms (e.g., anxiety, depression, spiritual distress). 17

19 PN2.4 The palliative care team uses physical and occupational therapy resources to optimize the child s function and mobility. PN2.5 Formal caregivers adjust the child s fluid and nutritional intake to accommodate changes in the child s ability to swallow and retain fluids in the intravascular space as well as changes in renal and hepatic function and other quality of life issues. PN2.6 The child s sensory experiences of sight, hearing, touch, taste and smell are optimized. PN2.7 The most effective, least invasive, evidence-based pain and symptom care interventions are used, based on the child s needs, to provide comfort, connection and communication between the ill child and his or her family, friends/peers and community. PN2.8 Complementary non-pharmacological symptom management techniques (e.g., music, art, books, journaling, guided imagery, clown therapy and play, hypnosis) are offered when appropriate, based on the assessment of the child s needs and interests. PN2.9 Formal caregivers who do not have the knowledge to ensure a child is as pain and symptom free as possible refer the child/family to specialized pediatric hospice palliative pain and comfort management services. These consultations may occur throughout the illness trajectory (i.e., when the focus of care is active, palliative or end of life/terminal). When this expertise is not available locally, formal caregivers use telephone or other means to consult with an appropriate service. PN2.10 All interventions and their effectiveness are documented and the data used to inform care decisions. PN2.11 Team members are involved in observing, evaluating and documenting symptom management interventions and their effectiveness. PN2.12 Formal caregivers receive ongoing education/training in pain and symptom assessment and management, including recognizing cues and feedback, and adjusting/evaluating symptom management strategies. 18

20 3. Psychosocial Care Principles PP3.1 PP3.2 Pediatric hospice palliative care addresses the psychological well-being of the child and family, and takes into account the emotional, cognitive, and behavioral impact of the illness, and each family member s personality, coping strategies, and past experiences. Hospice palliative care for children and their families depends on a holistic collaborative approach to spiritual, social, cultural, and psychological care. Norms of Practice PN3.1 The child/family s emotional well being is assessed. Formal caregivers ask the child and family about their specific thoughts, feelings, hopes, wishes, fears and memories, and develop an awareness of the child s and family s psychological expectations and needs, and their personalities, emotional status, coping strategies, cultural beliefs, past experiences, and any pre-existing psychological conditions. PN3.2 The plan of care addresses psychosocial needs and provides emotional support and therapies that promote the child s and family s coping skills and positive adjustment, supports their achievement of personal goals, and optimizes their quality of life. PN3.3 Feelings of anxiety, depression, anger, anticipatory grief, helplessness, and hopelessness are acknowledged and addressed, taking into account the child s level of development and the family s cultural beliefs. PN3.4 The child s cognitive function is preserved and developed as much as possible. PN3.5 The child s sense of independence and control are supported. PN3.6 Formal caregivers support the child s and family s desire for intimacy, privacy, connection and physical contact. PN3.7 Formal caregivers address the child s fears, sense of being a burden and desire to protect their family, as well as the child s and family s feelings of grief (e.g., loneliness, unresolved guilt, anger, hopelessness), taking into account the child s stage of development and the family s cultural beliefs. PN3.8 Formal caregivers strive to ensure that the child and family have opportunities for personal growth, joy and celebration. The care plan includes occasions for education, play, and interaction with family and peers, as well as other developmentally appropriate activities. Legacy building may be important (Hockley, 2000). PN3.9 The child s and family s dignity is preserved 19

21 PN3.10 Formal caregivers provide psychological care for the family during the bereavement process. If families ask for/require more bereavement support, they are offered referrals to community resources. 20

22 4. Social Care Principles PP4.1 PP4.2 PP4.3 Pediatric hospice palliative care is offered in a social context, and is based on an understanding of the child s and family s place in a network of extended family, friends, and community and the implications for interaction, communication, and decision-making with and within the family. Pediatric hospice palliative care takes into account relationship and communication issues within the extended family, the health-care setting, and the family s communities, including the need for assistance with conflict resolution. Pediatric hospice palliative care is culturally sensitive, and takes into account the beliefs, values, actions, customs, and the unique health care needs of the child and family. Norms of Practice PN4.1 PN4.2 PN4.3 PN4.4 PN4.5 PN4.6 PN4.7 Formal caregivers develop a non-judgmental awareness of the family s social context through a formal assessment as well as through conversations with the child and family. Formal caregivers ask the child and family about family relationships, available support systems, and resources, and share what they learn with other members of the team. The plan of care addresses the social expectations and needs of the child and family, and strives to support the importance, meaning and role of each person involved with the child. The child and family are supported in reconciling relationships as desired. When relationships are irreconcilable, the focus becomes healing and forgiveness. When desired by the family, formal caregivers educate and support the child s and family s network of extended family, friends and community as appropriate. Formal caregivers strive to create/maintain an environment that is safe and comforting, provides ample opportunity for communication, intimacy and privacy, supports family relationships, and supports the family/caregiver therapeutic relationship. Formal caregivers appreciate the intense physical, emotional, social and economic demands placed on a family caring for a child at home, or during prolonged and/or repeated hospitalizations. The family s ability to meet these demands with existing resources is assessed. (Hockley, 2000) Formal caregivers are aware of the potential impact of cultural diversity on interaction, communication, and decision-making and have access to cultural profiles that help them understand child and family preferences (e.g., in some cultures truth-telling is a means 21

23 PN4.8 of empowering the patient, while other cultures perceive truth-telling as robbing the individual of hope) (Candibet al, 2002). Formal caregivers ask the child and family about their own unique beliefs, values, and practices, and attempt to harmonize the beliefs and practices of the health-care system with those of the child and family, without causing stress for the child. Consultation is available to family and formal caregivers when there is a conflict based on cultural values and beliefs. 22

24 5. Spiritual Care Principles PP5.1 Spiritual care supports the child s and family s sense of: hope and self-worth; meaning and purpose; interconnectedness with others; and connection to powers larger than themselves. PP5.2 Individual family members may differ in their adherence to religious or spiritual practices. Norms of Practice PN5.1 PN5.2 PN5.3 PN5.4 PN5.5 Formal caregivers ask about the child s and family s beliefs and values, and determine what distinguishes spiritual from religious practice for the child and family, and share this information with the rest of the team. Formal caregivers acknowledge and respect the things that are meaningful and valuable to the child and family. The plan of care addresses the child s and family s spiritual expectations and needs, including any potential for conflict. Formal caregivers address the child s and family s existential questions and spiritual issues (e.g., the child dying before the parent) if able or make referrals to spiritual counsellors. Formal caregivers help the child and family access appropriate spiritual and/or religious resources, preferably those already known to the family. Where possible, personal spiritual advisors become part of the child s care team 23

25 6. Developmental Care Principles PP6.1 PP6.2 PP6.3 PP6.4 Children and adolescents are in a process of physical, emotional, cognitive and spiritual development. Depending on their developmental stage, they have different skills and different emotional, physical and development issues/needs. Children and adolescents communicate differently, and their understanding of illness, death and dying depends on their stage of development and their experience with death (e.g., pets, loved ones). Their concepts of illness and dying continue to evolve over time, and develop in association with life and illness experience. Learning is an essential integral part of children s lives. Education opportunities are incorporated into their dying journey if they desire. In families experiencing the death of a child, the child and his/her siblings may exhibit behaviours above or below the norms associated with their age, stage and illness/condition. Pediatric hospice palliative care provides care and support that is adapted to the children s developmental needs. Norms of Practice PN6.1 PN6.2 PN6.3 PN6.4 PN6.5 The child and his/her siblings developmental needs are assessed and addressed in the family-centred plan of care (see the growth and development charts in Appendix #). Formal caregivers adapt care to support the children s development.. Schooling is arranged to meet the needs of the child and/or siblings where possible, and children have opportunities to socialize with their peers. Parents receive guidance and support in their efforts to parent a child with a life limiting condition. If the child has difficulty communicating, formal caregivers identify a variety of verbal, nonverbal, and/or symbolic methods appropriate to the child s developmental level and communication style (see Appendix #). 24

26 7. Practical Care Principle PP7.1 Practical care, including assistance with activities of daily living and caregiver support, is an integral part of pediatric hospice palliative care. The child s and family s practical needs must be met to ensure quality of life. Norms of Practice PN7.1 PN7.2 PN7.3 PN7.4 PN7.5 PN7.6 The plan of care identifies the community and other resources required to address the child s and family s practical expectations and needs related to such areas as activities of daily living and caregiver support. The family s need for assistance with physical care of the child is addressed. The family s equipment and supply needs are addressed. The family s need for financial support for the child's care is addressed. The family s need for support, relief and respite is addressed. Families are referred to home care, respite services, volunteer visiting, hospices, long term care facilities and community support groups as appropriate, and have support coordinating the services and resources they need. Informal caregivers are trained and supported by the interdisciplinary team. 25

27 8. End of Life/Preparation for Death Care Principles PP8.1 Preparation for death, taking into account each child and family s unique needs, can be healing and is an integral part of pediatric hospice palliative care. Norms of Practice PN8.1 PN8.2 PN8.3 PN8.4 PN8.5 PN8.6 PN8.7 PN8.8 PN8.9 The plan of care helps children and families prepare for and manage the child s end of life and death. Symptoms and physiological changes associated with the last hours of living and death are anticipated, discussed with the child and family in a way that reflects their ability to cope with the information, and managed effectively. Decisions about advance care planning, including conversations regarding a possible autopsy, are clearly articulated and reviewed with the family Formal caregivers provide information about organ and tissue donation, and are available to discuss these issues at the family s request. The child and family are encouraged to prepare for death by participating in rites and rituals that are important to the family, and/or in life closure, gift giving, legacies and other meaningful activities if desired. Formal caregivers offer to provide assistance with or suggestions for a funeral, memorial or other meaningful services/celebrations of life if desired by the child and family. The family is offered grief support as well as grief and bereavement materials to help prepare for a child's death. The child s death is determined (i.e., pronounced), documented and communicated in accordance with regulation, policies and laws. The child s body is handled with respect and dignity in accordance with the wishes of the child and family. The family is given time with the deceased child. 26

28 9. Loss, Grief, Bereavement Care Principles PP9.1 PP9.2 PP9.3 PP9.4 PP9.5 Loss, grief and bereavement care is delivered in the context of wellness not pathology. Death, even the death of a child, is a normal part of life, and grief is a normal response to loss. Pediatric hospice palliative care focuses on: identifying the family s strengths; mobilizing personal, family, social and community resources; and providing emotional, practical, social and spiritual support (not treatment) for people experiencing grief and bereavement. Positive emotions and states of mind promote well-being and adjustment in bereavements (Bonnano et al, 2005). Loss, grief and bereavement care includes: a compassionate acknowledgement of the child's death, a bereavement care plan based on an assessment of the family s strengths and needs, emotional and practical support, and help accessing other community resources. The relationships that families develop with the child s formal caregivers and the family s experience of illness have a profound impact on their subsequent experience of death and bereavement. The family s grieving process will extend over many months or even years. Family members may experience a range of grief responses, and will require appropriate support to meet their needs. Some may benefit from referrals for counselling and appropriate treatment or alternative therapeutic approaches.. Pediatric hospice palliative care supports the family in creating/performing rituals that give unique personal meaning to the experience of illness, death and bereavement and respect the family s culture and preferences. Norms of Practice PN9.1 PN9.2 PN9.3 Families of children with progressive life-threatening illnesses have access to the services of hospital and community professionals with specialized expertise in grief and bereavement care. These professionals may become involved with a family at any point in their illness experience, depending on the family s preference and need. Following the death of a child, family members are offered bereavement care including: information, peer support, support from trained volunteers, support groups and support/counselling from bereavement care professionals. A bereavement care plan is developed based on an assessment of the family s strengths and needs and discussions with the family. Formal caregivers support the patient and family in their grieving process by, for example, having ongoing contact with the family, and acknowledging the child s birthday or the anniversary of the child s death. 27

29 PN9.4 Formal caregivers offer families a variety of supports and resources to address the ongoing physical, emotional and spiritual needs associated with loss and grief including, but not limited to: de-briefing sessions help planning/preparing for funeral services, burial ceremonies and/or other culturally appropriate rituals bereavement counselling referrals to community bereavement services support accessing grief and bereavement resources in hospital, home and community settings (e.g., support groups, peer support and trained volunteers). PN9.5 Community cultural leaders may be asked to participate in loss, grief and bereavement care. PN9.6 The responsibility for providing quality bereavement care is assumed by a member of the care team who has developed a relationship with the family and who is skilled in grief and bereavement care. PN9.7 Families are offered ongoing bereavement support/contact for a minimum of one year. Formal caregivers acknowledge the death and offer condolences two to three days after the death occurs, and contact families by phone or letter two to four weeks after the child's death and at appropriate times over the year to provide support and information. PN9.8 Team members have access to guidelines to help them provide appropriately, timely, evidence-based follow up contact with families. PN9.9 Individuals who indicate a need are offered access to grief counselling. PN9.10 Formal caregivers receive education and support to help them: develop the knowledge, skills and attitudes that foster quality bereavement care; assess family needs; and identify individuals who need more support/counselling. PN9.11 Formal caregivers working with children and families who face progressive, lifethreatening illness are offered grief and bereavement support as a regular part of staff support and on an as-needed basis (e.g., debriefing difficult deaths). 28

30 II. The Process of Providing Care The process of providing care consists of 6 steps or functions: assessment information sharing decision making therapeutic interventions care delivery (including interdisciplinary team care and continuity of care) evaluation/confirmation of care 10. Assessment Principles PP10.1 PP10.2 PP10.3 Assessment guides the clinician in understanding the child s experience of his or her illness/condition. Assessment and reassessment are comprehensive, interdisciplinary and timely so clinicians have adequate information to guide the plan of care. The assessment is supported by appropriate documentation. Norms of Practice PN10.1 Assessors gather appropriate information about the child s and family s history, respecting their privacy and using reliable assessment techniques and tools. Assessment information is shared with team members. PN10.2 History taking and physical examination are completed initially and at regular intervals (depending on child s condition) to ensure formal caregivers have adequate information to guide the plan of care. PN10.3 The initial assessment may take one or more visits and involve one or more formal caregivers (depending on their expertise. It includes: the physical examination and history taking, including symptoms identifying and prioritizing issues (expectations and needs) important to the child, family, and caregivers assessing the child s and family s developmental level, personal, cultural and spiritual values, beliefs and practices 29

31 assessing family structure, life/environmental context, family strengths, and family support PN10.4 The child s and family s perspectives are incorporated into the assessments of new and ongoing issues. PN10.5 Based on the assessment, the appropriate formal caregivers suggest laboratory tests, diagnostic studies and participation in clinical research when they have the potential to benefit the child without undue risk or burden. 30

32 11. Information-sharing Principles PP11.1 The child has the right to be informed about: his or her condition/illness, available treatment options and clinical trials, and their potential benefits, risks and burdens. The child also has the right to be invited to participate in decision making, depending on the child s stage of development and the family s cultural beliefs. PP11.2 Parents/substitute decision makers, with the guidance of professionals, determine how, when, and what information is shared with the child, taking into account the specific child, family and situation characteristics, such as temperament, cognitive abilities, developmental level, cultural beliefs and values. PP11.3 Parents/substitute decision makers are entitled to information about: the child s disease or condition; available treatment options and their potential benefits, risks and burdens; and palliative care. PP11.4 Effective communication and information sharing with the child and family gives formal caregivers the information they need to provide effective care. Norms of Practice PN11.1 Before sharing information, formal caregivers establish limits of privacy as defined by the child and family, and establish what the child and family already know and what they would like to know, in accordance with the ethical principle of truth telling. PN11.2 Accurate information is shared in a timely way and when the recipients are ready to receive it. PN11.3 Formal caregivers explore the expressive functioning/communication styles within the family, how family members normally share information, and any beliefs that may keep them from speaking with one another about difficult emotions / fears / worries. PN11.4 Information is shared in a language, manner and setting understandable and acceptable to the child and family. PN11.5 Interpretation services are provided by skilled medical interpreters who understand medical concepts and terminology, rather than by family members or someone who speaks the language. PN11.6 Formal caregivers regularly assess the child s and family s understanding and reactions to information, and their desire for additional information. PN11.7 When the family and formal caregivers disagree about information to be shared with the child, they use the principles of negotiation and conflict resolution to reach agreement. If they cannot reach agreement, they have access to the services of a people with expertise in conflict resolutions (e.g., child advocate, ethicist). 31